Search Thermo Fisher Scientific
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TGTTCCCGACAGGTACGGCTGCCAC[A/G]GAAGTTGGTGAGACCATTAGCTTCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612047 | ||||||||||||||||||||
Literature Links: |
E2F8 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
E2F8 - E2F transcription factor 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256371.1 | 2640 | Silent Mutation | TCC,TCT | S,S 706 | NP_001243300.1 | |
NM_001256372.1 | 2640 | Silent Mutation | TCC,TCT | S,S 706 | NP_001243301.1 | |
NM_024680.3 | 2640 | Silent Mutation | TCC,TCT | S,S 706 | NP_078956.2 | |
XM_011520367.1 | 2640 | Silent Mutation | TCC,TCT | S,S 601 | XP_011518669.1 |